Zhang Fuqiang, Hu Boyang, Fu Huiru, Jiao Zexin, Li Qi, Liu Shikai
Key Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China, Qingdao, China.
Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.
Front Genet. 2019 Jun 28;10:610. doi: 10.3389/fgene.2019.00610. eCollection 2019.
Fast growth is one of the most desired traits for all food animals, which affects the profitability of animal production. The Pacific oyster, , is an important aquaculture shellfish around the world with the largest annual production. Growth of the Pacific oyster has been greatly improved by artificial selection breeding, but molecular mechanisms underlying growth remains poorly understood, which limited the molecular integrative breeding of fast growth with other superior traits. In this study, comparative transcriptome analyses between the fast-growing selectively bred Pacific oyster and unselected wild Pacific oysters were conducted by RNA-Seq. A total of 1,303 protein-coding genes differentially expressed between fast-growing oysters and wild controls were identified, of which 888 genes were expressed at higher levels in the fast-growing oysters. Functional analysis of the differentially expressed genes (DEGs) indicated that genes involved in microtubule motor activity and biosynthesis of nucleotides and proteins are potentially important for growth in the oyster. Positive selection analysis of genes at the transcriptome level showed that a significant number of ribosomal protein genes had undergone positive selection during the artificial selection breeding process. These results also indicated the importance of protein biosynthesis and metabolism for the growth of oysters. The alternative splicing (AS) of genes was also compared between the two groups of oysters. A total of 3,230 differential alternative splicing events (DAS) were identified, involved in 1,818 genes. These DAS genes were associated with specific functional pathways related to growth, such as "long-term potentiation," "salivary secretion," and "phosphatidylinositol signaling system." The findings of this study will be valuable resources for future investigation to unravel molecular mechanisms underlying growth regulation in the oyster and other marine invertebrates and to provide solid support for breeding application to integrate fast growth with other superior traits in the Pacific oyster.
快速生长是所有食用动物最理想的性状之一,它影响着动物养殖的效益。太平洋牡蛎是全球重要的水产养殖贝类,年产量最高。通过人工选择育种,太平洋牡蛎的生长性能有了很大提高,但生长的分子机制仍知之甚少,这限制了快速生长与其他优良性状的分子综合育种。本研究通过RNA测序对快速生长的选育太平洋牡蛎和未选育的野生太平洋牡蛎进行了比较转录组分析。共鉴定出1303个在快速生长牡蛎和野生对照之间差异表达的蛋白质编码基因,其中888个基因在快速生长牡蛎中表达水平较高。对差异表达基因(DEGs)的功能分析表明,参与微管运动活性以及核苷酸和蛋白质生物合成的基因对牡蛎生长可能具有重要意义。转录组水平的基因正选择分析表明,在人工选择育种过程中,大量核糖体蛋白基因经历了正选择。这些结果也表明了蛋白质生物合成和代谢对牡蛎生长的重要性。还比较了两组牡蛎之间基因的可变剪接(AS)。共鉴定出3230个差异可变剪接事件(DAS),涉及1818个基因。这些DAS基因与特定的生长相关功能途径有关,如“长时程增强”、“唾液分泌”和“磷脂酰肌醇信号系统”。本研究结果将为未来揭示牡蛎和其他海洋无脊椎动物生长调控分子机制的研究提供宝贵资源,并为太平洋牡蛎快速生长与其他优良性状整合的育种应用提供坚实支持。